A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14463392



Internal ID22215899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145693712..145694599hg38UCSC Ensembl
chr4:146614864..146615751hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38888
hg19888
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3545366
Supporting Variants
SamplesHG00733
Known GenesC4orf51
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14463392
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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